日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Female reproductive tract-on-a-chip for selecting sperm with ultra-low DNA fragmentation index.

用于筛选DNA碎片指数超低的精子的女性生殖道芯片。

Dai Jing, Shan Han, Gu Yifan, Zheng Mingde, Lou Li, Xie Pingyuan, Zhang Shen, Sun Zheng, Gong Fei, Lu Guangxiu, Lin Ge, Chen Zeyu

Preclinical efficacy and safety evaluation of human embryonic stem cell-derived functional hepatocytes for a clinical trial in acute liver failure

人胚胎干细胞衍生功能性肝细胞治疗急性肝衰竭的临床前疗效和安全性评估

Sun, Yi; Yu, Juan; Shi, Yang; Wang, Yang; Duan, Xingxiang; Xie, Menghan; Ouyang, Qi; Zhao, Yan; Wang, Mei; Zhou, Baicun; Xu, Caiyun; Lu, Guangxiu; Lin, Ge

RNA-Seq of Cultured Peripheral Blood Lymphocytes Improves Identification of Cryptic Splicing Defects in Rare Disease Diagnostics

培养的外周血淋巴细胞的RNA测序提高了罕见病诊断中隐匿性剪接缺陷的识别率

Ren, Jinlin; Dai, Congling; Meng, Fei; Zhang, Pan; Xie, Chunbo; Xiao, Wenjuan; He, Wenbin; Yuan, Shimin; Li, Xiurong; Zhang, Qianjun; Tang, Weiling; Hu, Liang; Chen, Zixu; Lu, Guangxiu; Du, Juan; Zeng, Sicong; Lin, Ge

A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnostics

非梗阻性无精子症的常见病因:MEI1双等位基因变异及其对不孕症诊断的意义

Tan, Chen; Wang, Tiantian; Tu, Chaofeng; Xie, Chunbo; Chen, Zixu; Yuan, Shimin; Hu, Tongyao; He, Wenbin; Li, Yong; Wang, Yurong; Luo, Chen; Zhang, Qianjun; Nie, Hongchuan; Zhang, Huan; Lu, Guangxiu; Lin, Ge; Tan, Yue-Qiu; Meng, Lanlan; Du, Juan

Genetic rare disease prevention and control: Family-based screening and reproductive interventions in Changsha

遗传罕见病防控:长沙市基于家庭的筛查和生殖干预

Lin, Ge; He, Jun; Wang, Yuankun; Liu, Xiangyan; Du, Juan; Zhang, Qianjun; Zhou, Shihao; Hu, Lanping; He, Jing; Li, Xiurong; Hu, Hao; Hu, Liang; Zhong, Changgao; He, Wen-Bin; Peng, Chan; Xu, Zhen; Zhang, Jingjing; Shu, Yan; Song, Xuan; Zhang, Wenqian; Lu, Guangxiu; Ou, Zhiming; Tan, Yue-Qiu; Liu, Jiyang

SARS-CoV-2 infection is detrimental to pregnancy outcomes after embryo transfer in IVF/ICSI: a prospective cohort study

SARS-CoV-2感染对体外受精/卵胞浆内单精子注射(IVF/ICSI)胚胎移植后的妊娠结局有不利影响:一项前瞻性队列研究

Li, Yuan; Zhao, Qi; Ma, Shujuan; Tang, Sha; Lu, Guangxiu; Lin, Ge; Gong, Fei

Extended application of PGT-M strategies for small pathogenic CNVs

PGT-M策略在小型致病性CNV中的扩展应用

Hu, Xiao; Wang, Weili; Luo, Keli; Dai, Jing; Zhang, Yi; Wan, Zhenxing; He, Wenbin; Zhang, Shuoping; Yang, Lanlin; Tan, Qin; Li, Wen; Zhang, Qianjun; Gong, Fei; Lu, Guangxiu; Tan, Yue-Qiu; Lin, Ge; Du, Juan

Homozygous ACTL9 mutations cause irregular mitochondrial sheath arrangement and abnormal flagellum assembly in spermatozoa and male infertility.

ACTL9 纯合突变会导致精子线粒体鞘排列异常和鞭毛组装异常,从而导致男性不育

Li Qi, Huang Yilian, Zhang Shen, Gong Fei, Lu Guangxiu, Lin Ge, Dai Jing

Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression

人类C12orf40基因的功能缺失变异会阻断减数分裂进程,从而导致男性不育。

Tu, Chaofeng; Wen, Junfei; Wang, Weili; Zhu, Qifan; Chen, Ying; Cheng, Jianglu; Li, Zeye; Meng, Lanlan; Li, Yong; He, Wenbin; Tan, Chen; Xie, Chunbo; Fu, Shao-Mei; Du, Juan; Lu, Guangxiu; Lin, Ge; Gou, Lan-Tao; Tan, Yue-Qiu

Single-cell transcriptome analysis of NEUROG3+ cells during pancreatic endocrine differentiation with small molecules

利用小分子对胰腺内分泌分化过程中 NEUROG3+ 细胞进行单细胞转录组分析

Li, Jin; Chen, Junru; Luo, Xiaoyu; Lu, Guangxiu; Lin, Ge